Forum Discussion
KatieT
9 years agoMember
Hair Loss is not always temporary
I have been scouring the internet looking for suggestions or therapies to improve my sad head of hair.
All the websites say the same thing as the BCNA fact sheet or similar, "Remember that hair loss is temporary".
I really think this is misrepresenting the situation to a percentage of women going through breast cancer treatment. Some women are told this by their oncologists, their support nurses and their families ... and then it's not true. Some don't get any hair back. Some get a small amount of thin wispy hair back in some places on their head.
https://www.bcna.org.au/sites/default/files/bcna-fact-sheet-hair-loss-during-breastcancer-treatment.pdf
Why not tell women at the beginning of their treatment that this could seriously impact on their physical appearance perhaps forever. Then don't minimize their anxiety about it by telling them it's not real or it's temporary. For some it is. For some it isn't.
My suggestion to oncologists and medical support practitioners is tell women the possibilities and then let them choose the treatment or not. Don't tell them it will grow back if it's a known possible side affect for hair to be partially or radically permanently affected by the treatments.
Maybe BCNA could play a role in getting some real information available for women. I'm looking for therapies or treatments, anything that can help me look like a normal middle-aged woman instead of an unwell senior citizen. I haven't found anything yet and there must be other women out there like me searching for the same thing.
All the websites say the same thing as the BCNA fact sheet or similar, "Remember that hair loss is temporary".
I really think this is misrepresenting the situation to a percentage of women going through breast cancer treatment. Some women are told this by their oncologists, their support nurses and their families ... and then it's not true. Some don't get any hair back. Some get a small amount of thin wispy hair back in some places on their head.
https://www.bcna.org.au/sites/default/files/bcna-fact-sheet-hair-loss-during-breastcancer-treatment.pdf
Why not tell women at the beginning of their treatment that this could seriously impact on their physical appearance perhaps forever. Then don't minimize their anxiety about it by telling them it's not real or it's temporary. For some it is. For some it isn't.
My suggestion to oncologists and medical support practitioners is tell women the possibilities and then let them choose the treatment or not. Don't tell them it will grow back if it's a known possible side affect for hair to be partially or radically permanently affected by the treatments.
Maybe BCNA could play a role in getting some real information available for women. I'm looking for therapies or treatments, anything that can help me look like a normal middle-aged woman instead of an unwell senior citizen. I haven't found anything yet and there must be other women out there like me searching for the same thing.
38 Replies
- GlemmisMemberI have just finished AC & will be starting Paclitaxol & my oncologist said she wouldn't use the other drug as it is unacceptable for women to not have their hair grow back.
- socodaMemberKatie, Wishing you all the best and hoping you see massive improvements in your hair growth. Xx
- KatieTMemberI went to the hair clinic for a free appointment. The consultant there seemed to know nothing about the effects of chemotherapy on the scalp but he still thought his treatments could help me. I asked whether he'd ever treated anybody before or had any published research on it but the answer was no to both. It was going to cost $4500 for a 12 month program of laser treatments, minixidil solution and other hair tonics. I decided I couldn't justify the money with no guarantees and no research.
So my plan now is keep on the Minoxidil. I have found I can buy it on ebay a lot cheaper and also in a higher dosage which is appropriate for me apparently. I have also joined the ranks of the desperate and gullible and bought a laser treatment helmet calls an iGrow. I found one secondhand for $300. I use the lasers for 25 mins each day but have only just started that.
On the Minoxidil, I have now been using it for 3 months and recently upped from the 2% to the 5%. I am seeing some improvement in the areas of application I think. I have some young hairs coming through there that are about 2cm long now. There's a sort of fluffy feel to the area too and I suspect there may be more coming. I am putting the medication in the thin areas on top, at the crown, at the temples and on my forehead. I really hope the little bit of improvement I've started to notice continues. - PaulaNMemberI lost my hair from taking anastrozole in June. Now it looks like I'v had a short (if you can) crew cut. Its grown back a lot darker but seems to come to a stand still. I was changed to letrozole but nothings changed, so I guess at this stage its a good thing
- KatieTMemberI haven't tried that. I have tried Coconut oil and Moroccan oil. Bio-oil and about four other oils. My hair sucks up oil like a sponge. I drench it at night and in the morning it feels dry again. I've never experienced anything like it. I think it's because my hair follicles probably aren't exuding any oil. I will give it a try. It can't hurt.
- Ro10Member@KatieT you've probably tried everything already but someone mentioned to me yesterday to use cold pressed castor oil. Apparently it is quite good to stimulate hair growth and can be applied directly to the scalp.
- KatieTMemberMy oncologist thinks nothing like that is an issue and it's just the chemotherapy damage. I asked him what I should do now and he said there's no medical treatments and perhaps a hair clinic might be the next thing. I have an appointment with Advanced Hair Studio later this week. I am not sure what they can tell me but I'm going to go anyway. I suspect they won't know anything about damage from Docetaxel as nobody seems to, but they might be able to assess the real condition of the hair follicles and tell me if anything can be improved or if I can try anything. Perhaps they can spot any signs of other issues. I don't know but I will find out. I have no history of stress-related hair loss or alopecia prior to this.
Hi Katie, I had 4 x AC and 12 x Taxol, but my hair is now starting to grow back. But I was thinking, maybe it would be good to rule out other causes of hair loss, for example alopecia, which I think can be stress or immune system related, and not necessarily permanent. I guess maybe a dermatologist or maybe an immunotherapist might be able to advise? Just a thought, as it might be coincidental to the chemo rather than a result of it.
Good on you for bringing this to our attention. I hope you can find some answers.
- Ro10MemberThanks for this info @primek I was getting a bit worried that I would have permanent hair loss and this definitely has not been mentioned to me. In fact, the nurse giving me the chemo actually said that like you, a lot of people have their hair grow back while doing the weekly paclitaxel treatment
- AfraserMemberSo did mine, equally surprised as I had assumed nothing would happen until I had finished.